Cisplatin versus carboplatin: comparative review of therapeutic management in solid malignancies

被引:237
作者
Ho, Gwo Yaw [1 ,2 ,4 ]
Woodward, Natasha [2 ]
Coward, Jermaine I. G. [1 ,2 ,3 ]
机构
[1] Univ Queensland, Sch Med, Brisbane, Qld 4072, Australia
[2] Mater Hlth Serv, Raymond Terrace, South Brisbane, Qld 4101, Australia
[3] Princess Alexandra Hosp, Ipswich Rd, Woolloongabba, Qld 4102, Australia
[4] Walter & Eliza Hall Inst Med Res, 1G Royal Parade, Parkville, Vic 3052, Australia
关键词
Cisplatin; Carboplatin; Radio-sensitisation; Platinum-based chemotherapy; Platinum resistance; Platinum sensitivity; PHASE-III TRIAL; UNKNOWN PRIMARY SITE; RECURRENT ENDOMETRIAL CARCINOMA; PEMETREXED PLUS CARBOPLATIN; TRANSITIONAL-CELL CARCINOMA; NUCLEOTIDE EXCISION-REPAIR; MESSENGER-RNA EXPRESSION; LOCALLY ADVANCED HEAD; RANDOMIZED-TRIAL; OVARIAN-CANCER;
D O I
10.1016/j.critrevonc.2016.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The platinum analogues, cisplatin and carboplatin, are among the most widely used chemotherapeutic agents in oncology. Both agents have a broad spectrum of clinical activity in numerous malignancies including gynaecological cancers, germ cell tumours, head and neck cancer, thoracic cancers and bladder cancer. Although the final mechanism of inducing tumour cell apoptosis is similar for both compounds, cisplatin has been shown to be more effective in treating specific tumour types. Whilst more favourable toxicity profiles are often associated with carboplatin, this can frequently translate to inferior response in certain malignancies. This review succinctly collates the evidence for the preferential use of these platinum analogues in particular settings in addition to the long-standing dilemma surrounding the paucity of biomarkers predicting response to these agents. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:37 / 46
页数:10
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